Canonical Allele Identifier: CA381981333

Gene: ACER3

Linked Data

• ClinVar Variation Id: 446204
• ClinVar RCV Id: RCV000515460 ; RCV001851412
• dbSNP Id: rs1554988032
• MyVariant Identifiers: chr11:g.76572118A>G (hg19) ; chr11:g.76861074A>G (hg38)
• PubMed: PMID:26792856

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.76861074A>G , CM000673.2:g.76861074A>G	GRCh38
NC_000011.9:g.76572118A>G , CM000673.1:g.76572118A>G	GRCh37
NC_000011.8:g.76249766A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530182.6:n.140A>G
ENST00000530334.6:c.98A>G	ENSP00000435048.2:p.Glu33Gly
ENST00000532485.6:c.98A>G MANE Select	ENSP00000434480.1:p.Glu33Gly
ENST00000679611.1:n.138A>G
ENST00000679754.1:c.98A>G	ENSP00000505416.1:p.Glu33Gly
ENST00000679866.1:c.98A>G	ENSP00000505175.1:p.Glu33Gly
ENST00000679924.1:c.-66A>G	ENSP00000506405.1:n.-66A>G
ENST00000680583.1:c.-130+12A>G	ENSP00000505842.1:n.-130+12A>G
ENST00000680842.1:c.98A>G	ENSP00000506534.1:p.Glu33Gly
ENST00000681004.1:c.98A>G	ENSP00000505132.1:p.Glu33Gly
ENST00000681251.1:c.98A>G	ENSP00000505549.1:p.Glu33Gly
ENST00000681257.1:c.98A>G	ENSP00000506160.1:p.Glu33Gly
ENST00000681354.1:c.98A>G	ENSP00000505846.1:p.Glu33Gly
ENST00000681375.1:c.98A>G	ENSP00000506417.1:p.Glu33Gly
ENST00000681411.1:c.98A>G	ENSP00000504918.1:p.Glu33Gly
ENST00000681732.1:c.98A>G	ENSP00000504927.1:p.Glu33Gly
ENST00000681955.1:c.98A>G	ENSP00000505191.1:p.Glu33Gly
ENST00000278544.9:c.98A>G	ENSP00000278544.5:p.Glu33Gly
ENST00000525194.5:c.98A>G	ENSP00000432109.1:p.Glu33Gly
ENST00000525861.5:c.98A>G	ENSP00000432379.1:p.Glu33Gly
ENST00000526597.5:c.-254+12A>G	ENSP00000431149.1:n.-254+12A>G
ENST00000530182.5:n.154A>G
ENST00000530334.5:c.98A>G	ENSP00000435048.1:p.Glu33Gly
ENST00000531352.5:c.98A>G	ENSP00000431504.1:p.Glu33Gly
ENST00000531461.5:c.98A>G	ENSP00000433368.1:p.Glu33Gly
ENST00000532485.5:c.98A>G	ENSP00000434480.1:p.Glu33Gly
ENST00000533873.1:c.98A>G	ENSP00000436252.1:p.Glu33Gly
ENST00000534206.5:c.-24+12A>G	ENSP00000435733.1:n.-24+12A>G
NM_001300953.1:c.98A>G	NP_001287882.1:p.Glu33Gly
NM_001300954.1:c.-259A>G	NP_001287883.1:n.-259A>G
NM_001300955.1:c.-135A>G	NP_001287884.1:n.-135A>G
NM_018367.6:c.98A>G	NP_060837.3:p.Glu33Gly
XM_005274087.3:c.-177A>G	XP_005274144.1:n.-177A>G
XM_005274092.2:c.98A>G	XP_005274149.1:p.Glu33Gly
XM_011545151.1:c.98A>G	XP_011543453.1:p.Glu33Gly
XM_011545153.1:c.98A>G	XP_011543455.1:p.Glu33Gly
XR_949982.1:n.186A>G
XR_949983.1:n.186A>G
XR_949984.1:n.186A>G
XR_949985.1:n.186A>G
XM_011545151.2:c.98A>G	XP_011543453.1:p.Glu33Gly
XM_011545153.2:c.98A>G	XP_011543455.1:p.Glu33Gly
XM_017017987.1:c.98A>G	XP_016873476.1:p.Glu33Gly
XM_017017988.1:c.98A>G	XP_016873477.1:p.Glu33Gly
XR_001747918.1:n.168A>G
XR_001747919.1:n.168A>G
NM_018367.7:c.98A>G MANE Select	NP_060837.3:p.Glu33Gly
NM_001300953.2:c.98A>G	NP_001287882.1:p.Glu33Gly
NM_001300954.2:c.-259A>G	NP_001287883.1:n.-259A>G
NM_001300955.2:c.-135A>G	NP_001287884.1:n.-135A>G